NDC 70518-1559-2 - Clonazepam
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 70518-1559
- Requested NDC
- 70518-1559-2
- Package NDCs from labels
- 70518-1559-0, 70518-1559-2, 70518-1559-1
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2024-08-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Clonazepam Tablets, USP Rx only | REMEDYREPACK INC. | 2024-08-09 | HUMAN PRESCRIPTION DRUG LABEL |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Clonazepam | CLONAZEPAM | Aphena Pharma Solutions - Tennessee, LLC | c68420a9-b646-4a4f-99f7-43d652312eb0 | 2018-02-14 | Warnings, Adverse reactions | ANDA077147 197528 5PE9FDE8GB |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.